NCT07656311

Brief Summary

This study aims to investigate whether Mean Platelet Volume (MPV) and other blood count parameters measured at admission can predict mortality in cancer patients admitted to the intensive care unit (ICU). Patients with cancer are highly vulnerable to complications and organ failure, making early risk assessment vital for improving treatment strategies. Researchers will retrospectively review the medical charts and electronic health records of adult patients who stayed in the anesthesia ICU for longer than 24 hours between 2020 and 2025. No new laboratory tests, interventions, or patient contact will occur. The collected data will be analyzed to determine the relationship between initial MPV levels and patient survival outcomes.

Trial Health

55
Monitor

Trial Health Score

Automated assessment based on enrollment pace, timeline, and geographic reach

Trial has exceeded expected completion date
Enrollment
425

participants targeted

Target at P75+ for all trials

Timeline
Completed

Started Jun 2026

Shorter than P25 for all trials

Geographic Reach
1 country

1 active site

Status
enrolling by invitation

Health score is calculated from publicly available data and should be used for screening purposes only.

Trial Relationships

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Study Timeline

Key milestones and dates

First Submitted

Initial submission to the registry

June 15, 2026

Completed
Same day until next milestone

Study Start

First participant enrolled

June 15, 2026

Completed
3 days until next milestone

First Posted

Study publicly available on registry

June 18, 2026

Completed
1 month until next milestone

Primary Completion

Last participant's last visit for primary outcome

August 1, 2026

Completed
Same day until next milestone

Study Completion

Last participant's last visit for all outcomes

August 1, 2026

Completed
Last Updated

June 18, 2026

Status Verified

June 1, 2026

Enrollment Period

2 months

First QC Date

June 15, 2026

Last Update Submit

June 15, 2026

Conditions

Keywords

Mean Platelet VolumecancerIntensive Care UnitICU MortalityBiomarkersMPV

Outcome Measures

Primary Outcomes (1)

  • Intensive Care Unit (ICU) Mortality

    The percentage of oncological patients who died during their stay in the anesthesia intensive care unit. This will be calculated based on the electronic health records and patient files.

    From the date of ICU admission up to ICU discharge, assessed up to 30 days.

Secondary Outcomes (1)

  • Hospital Mortality

    From the date of hospital admission up to hospital discharge, assessed up to 60 days.

Study Arms (1)

Oncological ICU Patients

Adult patients (aged 18 and older) with a confirmed cancer diagnosis who were admitted to the anesthesia intensive care unit for longer than 24 hours between the years 2020 and 2025

Eligibility Criteria

Age18 Years+
Sexall
Healthy VolunteersNo
Age GroupsAdult (18-64), Older Adult (65+)
Sampling MethodNon-Probability Sample
Study Population

The study population consists of adult oncological patients who required critical care and were admitted to the anesthesia intensive care unit of a tertiary oncology training and research hospital between 2020 and 2025.

You may qualify if:

  • Adult patients aged 18 years and older.
  • Patients with a pathologically or clinically confirmed diagnosis of cancer (solid or hematological malignancies).
  • Patients who were admitted to the Anesthesia Intensive Care Unit (ICU) between 2020 and 2025.
  • Patients with an ICU length of stay longer than 24 hours.
  • Patients with complete medical records, including baseline complete blood count (CBC) and Mean Platelet Volume (MPV) measured at the time of ICU admission.

You may not qualify if:

  • Patients under the age of 18.
  • Patients who stayed in the intensive care unit for less than 24 hours.
  • Patients with missing or incomplete medical charts, laboratory data, or survival status records.
  • Patients who were readmitted to the ICU during the same hospital stay (only the first admission will be evaluated).
  • Patients who received massive blood or platelet transfusions immediately prior to the baseline laboratory measurement, which could artificially alter platelet parameters.

Contact the study team to confirm eligibility.

Sponsors & Collaborators

Study Sites (1)

Dr. Abdurrahman Yurtaslan Oncology Training and Research Hospital

Ankara, Turkey (Türkiye)

Location

MeSH Terms

Conditions

Critical IllnessNeoplasms

Condition Hierarchy (Ancestors)

Disease AttributesPathologic ProcessesPathological Conditions, Signs and Symptoms

Study Design

Study Type
observational
Observational Model
COHORT
Time Perspective
OTHER
Target Duration
30 Days
Sponsor Type
OTHER
Responsible Party
PRINCIPAL INVESTIGATOR
PI Title
Dr. Eda Cennet Caferoğlu

Study Record Dates

First Submitted

June 15, 2026

First Posted

June 18, 2026

Study Start

June 15, 2026

Primary Completion

August 1, 2026

Study Completion

August 1, 2026

Last Updated

June 18, 2026

Record last verified: 2026-06

Data Sharing

IPD Sharing
Will not share

Individual participant data will not be shared globally to maintain patient confidentiality and privacy in accordance with local data protection regulations and institutional review board restrictions. However, the coded datasets and statistical analyses used during the current study may be available from the corresponding author upon reasonable academic request.

Locations